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Patient self-management of oral anticoagulation with vitamin K antagonists in everyday practice: clinical outcomes in a single centre cohort after long-term follow-up

BMC cardiovascular disorders, 2020-04, Vol.20 (1), p.166-166, Article 166

2020

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Risk of a first venous thrombotic event in carriers of a familial thrombophilic defect. The European Prospective Cohort on Thrombophilia (EPCOT)

Journal of thrombosis and haemostasis, 2005-03, Vol.3 (3), p.459-464

2005

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Risk of ischemic stroke associated with functional thrombin-activatable fibrinolysis inhibitor plasma levels

Stroke (1970), 2003-10, Vol.34 (10), p.2387-2391

2003

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Genetic determinants of plasma β2‐glycoprotein I levels: a genome‐wide association study in extended pedigrees from Spain

Journal of thrombosis and haemostasis, 2013-03, Vol.11 (3), p.521-528

2013

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Genetic determinants of hemostasis phenotypes in spanish families

Circulation (New York, N.Y.), 2000-04, Vol.101 (13), p.1546-1551

2000

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Familial thrombophilia and lifetime risk of venous thrombosis

Journal of thrombosis and haemostasis, 2004-09, Vol.2 (9), p.1526-1532

2004

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Low-molecular-weight heparin as bridging therapy during interruption of oral anticoagulation in patients undergoing colonoscopy or gastroscopy

International journal of clinical practice (Esher), 2007-02, Vol.61 (2), p.212-217

2007

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Functional effects of the ABO locus polymorphism on plasma levels of von Willebrand factor, factor VIII, and activated partial thromboplastin time

Arteriosclerosis, thrombosis, and vascular biology, 2000-08, Vol.20 (8), p.2024

2000

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Hereditary thrombophilia and fetal loss: a prospective follow‐up study

Journal of thrombosis and haemostasis, 2004-04, Vol.2 (4), p.592-596

2004

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Linkage analysis demonstrates that the prothrombin G20210A mutation jointly influences plasma prothrombin levels and risk of thrombosis

Blood, 2000-05, Vol.95 (9), p.2780-2785

2000

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Low ADAMTS13 levels are associated with venous thrombosis risk in women

Thrombosis research, 2017-09, Vol.157, p.38-40

2017

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A locus on chromosome 2 influences levels of tissue factor pathway inhibitor: results from the GAIT study

Arteriosclerosis, thrombosis, and vascular biology, 2005-07, Vol.25 (7), p.1489

2005

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Antitumoral effect of maintained neutrophilia induced by rhG-CSF in a murine model of pancreatic cancer

Scientific reports, 2019-02, Vol.9 (1), p.2879-2879, Article 2879

2019

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Coagulation factor XII genetic variation, ex vivo thrombin generation, and stroke risk in the elderly: results from the Cardiovascular Health Study

Journal of thrombosis and haemostasis, 2015-10, Vol.13 (10), p.1867-1877

2015

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The prothrombin 20210A allele is the most prevalent genetic risk factor for venous thromboembolism in the Spanish population

Thrombosis and haemostasis, 1998-09, Vol.80 (3), p.366

1998

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Changes in cardiac biomarkers in goats naturally affected by pregnancy toxemia

Research in veterinary science, 2020-06, Vol.130, p.73-78

2020

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Association of complement receptor 2 polymorphisms with innate resistance to HIV-1 infection

Genes and immunity, 2015-03, Vol.16 (2), p.134-141

2015

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Genetic studies in complex disease: the case pro linkage studies

Journal of thrombosis and haemostasis, 2003-08, Vol.1 (8), p.1676-1678

Souto, J. C.

2003

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Risk of thrombosis associated with oral contraceptives of women from 97 families with inherited thrombophilia: high risk of thrombosis in carriers of the G20210A mutation of the prothrombin gene

Haematologica (Roma), 2001-09, Vol.86 (9), p.965

2001

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Prothrombotic state and signs of endothelial lesion in plasma of patients with inflammatory bowel disease

Digestive diseases and sciences, 1995-09, Vol.40 (9), p.1883-1889

1995

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Oral surgery in anticoagulated patients without reducing the dose of oral anticoagulant: A prospective randomized study

Journal of oral and maxillofacial surgery, 1996, Vol.54 (1), p.27-32

1996

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Recurrence rate after a first venous thrombosis in patients with familial thrombophilia

Arteriosclerosis, thrombosis, and vascular biology, 2005-09, Vol.25 (9), p.1992

2005

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Apixaban for the Treatment of Venous Thromboembolism Associated with Cancer

The New England journal of medicine, 2020-04, Vol.382 (17), p.1599-1607

2020

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A Genomewide Exploration Suggests a New Candidate Gene at Chromosome 11q23 as the Major Determinant of Plasma Homocysteine Levels: Results from the GAIT Project

American journal of human genetics, 2005-06, Vol.76 (6), p.925-933

2005

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Patient self-management of oral anticoagulation with vitamin K antagonists in everyday practice: clinical outcomes in a single centre cohort after long-term follow-up

Risk of a first venous thrombotic event in carriers of a familial thrombophilic defect. The European Prospective Cohort on Thrombophilia (EPCOT)

Risk of ischemic stroke associated with functional thrombin-activatable fibrinolysis inhibitor plasma levels

Genetic determinants of plasma β2‐glycoprotein I levels: a genome‐wide association study in extended pedigrees from Spain

Genetic determinants of hemostasis phenotypes in spanish families

Familial thrombophilia and lifetime risk of venous thrombosis

Low-molecular-weight heparin as bridging therapy during interruption of oral anticoagulation in patients undergoing colonoscopy or gastroscopy

Functional effects of the ABO locus polymorphism on plasma levels of von Willebrand factor, factor VIII, and activated partial thromboplastin time

Hereditary thrombophilia and fetal loss: a prospective follow‐up study

Linkage analysis demonstrates that the prothrombin G20210A mutation jointly influences plasma prothrombin levels and risk of thrombosis

Low ADAMTS13 levels are associated with venous thrombosis risk in women

A locus on chromosome 2 influences levels of tissue factor pathway inhibitor: results from the GAIT study

PDGFB, a new candidate plasma biomarker for venous thromboembolism: results from the VEREMA affinity proteomics study

Antitumoral effect of maintained neutrophilia induced by rhG-CSF in a murine model of pancreatic cancer

Coagulation factor XII genetic variation, ex vivo thrombin generation, and stroke risk in the elderly: results from the Cardiovascular Health Study

The prothrombin 20210A allele is the most prevalent genetic risk factor for venous thromboembolism in the Spanish population

Changes in cardiac biomarkers in goats naturally affected by pregnancy toxemia

Association of complement receptor 2 polymorphisms with innate resistance to HIV-1 infection

Genetic studies in complex disease: the case pro linkage studies

Risk of thrombosis associated with oral contraceptives of women from 97 families with inherited thrombophilia: high risk of thrombosis in carriers of the G20210A mutation of the prothrombin gene

Prothrombotic state and signs of endothelial lesion in plasma of patients with inflammatory bowel disease

Oral surgery in anticoagulated patients without reducing the dose of oral anticoagulant: A prospective randomized study

Recurrence rate after a first venous thrombosis in patients with familial thrombophilia

Apixaban for the Treatment of Venous Thromboembolism Associated with Cancer

A Genomewide Exploration Suggests a New Candidate Gene at Chromosome 11q23 as the Major Determinant of Plasma Homocysteine Levels: Results from the GAIT Project

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